Canonical Allele Identifier: PA2580107024
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1765710
ClinVar RCV Id: RCV002449976
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Leu303Met
CA345438432
NM_000143.4:c.907T>A